Human laminin β2 deficiency causes congenital nephrosis with mesangial sclerosis and distinct eye abnormalities
収録刊行物
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- Human Molecular Genetics
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Human Molecular Genetics 13 (21), 2625-2632, 2004-09-14
Oxford University Press (OUP)
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詳細情報 詳細情報について
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- CRID
- 1360011144964638464
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- NII論文ID
- 30018402956
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- ISSN
- 14602083
- 09646906
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